Improving identification of intimate partner violence in primary care

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to enhance the ability of primary care professionals to identify individuals exposed to intimate partner violence (IPV) through three different interventions. Participants will be randomized to use either a standardized questionnaire, tailored virtual patients for training, or a combination of both. The effectiveness of these interventions will be assessed by measuring the identification rates of IPV victims before and after the interventions, along with qualitative feedback from healthcare professionals. The project will take place over three years across various primary care settings, including health centers and youth clinics.

Why it matters

Who can join: the full rules

Inclusion criteria:

* All health care staff who meet patients at the included study sites are elegible for the study
* Midwives, MDs, psychologists, social workers, nurses etc.

Exclusion criteria:

\- Health care staff who does not want to participate

Where it's running

• Linköping University
  Linköping, Sweden Recruiting

Study contacts

• Principal investigator: Mia M Barimani, Professor — Linkoeping University
• Study coordinator: Mia Barimani, Professor
• Email: mia.barimani@liu.se
• Phone: 0046-73-7083163

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.